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Preparation of natural borneol/2-hydroxypropyl-β-cyclodextrin inclusion complex and its effect on the absorption of tetramethylpyrazine phosphate in mouse

机译:天然冰片/ 2-羟丙基-β-环糊精包合物的制备及其对四甲基吡嗪磷酸酯在小鼠体内吸收的影响

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Natural borneol (NB)/2-hydroxypropyl-β-cyclodextrin (HP-β-CD) inclusion complex has been prepared, and characterized by differential scanning calorimetry (DSC), X-ray diffractometry (XRD) and Fourier transform infrared spectroscopy (FT-IR). The phase solubility and release of NB, and its effect on the absorption of tetramethylpyrazine phosphate (TMPP) in mice were also measured. The results demonstrated that NB could be efficiently loaded into HP-β-CD to form an inclusion complex at a mass ratio of 1:6, and the inclusion complex had different physicochemical characteristics from free NB. The profile of phase solubility displayed a typical A _L-type, indicating the formation of 1:1 stoichiometric inclusion complex. Additionally, the stability of the inclusion complex was greatly improved compared with that of NB. The results of absorption of TMPP in mouse indicated that NB/HP-β-CD enhanced the absorption of TMPP and the concentration of TMPP in brain tissue, especially in the early period. Both TMPP plasma and brain concentration-time courses in mice were fitted to open two-compartment model with first-order absorption after oral administration of TMPP with NB/HP-β-CD. However, the use of NB/HP-β-CD did not change the in vivo behavior of TMPP. Our results suggest the application potential of NB/HP-β-CD inclusion in pharmaceutics.
机译:制备了天然冰片(NB)/ 2-羟丙基-β-环糊精(HP-β-CD)包合物,并通过差示扫描量热法(DSC),X射线衍射法(XRD)和傅里叶变换红外光谱(FT)进行了表征-IR)。还测量了NB的相溶解度和释放,以及其对小鼠四甲基吡嗪磷酸酯(TMPP)吸收的影响。结果表明,NB可以有效负载到HP-β-CD中,形成质量比为1:6的包合物,包合物的理化特性与游离NB不同。相溶解度曲线显示出典型的A _L型,表明形成了1:1化学计量的包合物。另外,与NB相比,包合物的稳定性大大提高。小鼠对TMPP的吸收结果表明,NB /HP-β-CD可增强TMPP的吸收和脑组织中TMPP的浓度,尤其是在早期。口服TMPP与NB /HP-β-CD口服后,小鼠中的TMPP血浆和脑浓缩时间过程均适合于建立具有一阶吸收的两室模型。但是,使用NB /HP-β-CD不会改变TMPP的体内行为。我们的结果表明,NB /HP-β-CD包涵体在药物中的应用潜力。

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